Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 THALASSAEMIA IN SCOTS.

Literature DB >> 14076382

THALASSAEMIA IN SCOTS.

K D BUCHANAN, J D KINLOCH, H E HUTCHISON, P H PINKERTON, P CASSIDY.

Abstract

Five cases of thalassaemia minor and 11 symptomless trait carriers have been detected in four Scottish families, only one of which is known to have foreign ancestry. It is suggested that the condition is commoner than was once thought, and that the diagnosis should be considered in any patient with refractory hypochromic anaemia in which the red cells show increased osmotic resistance.

Entities: Disease Species

Keywords: EPIDEMIOLOGY; ERYTHROCYTES; GENETICS, HUMAN; HEMOGLOBINOMETRY; OSMOSIS; SCOTLAND; THALASSEMIA

Mesh：

Year: 1963 PMID： 14076382 PMCID： PMC480647 DOI： 10.1136/jcp.16.6.596

Source DB: PubMed Journal: J Clin Pathol ISSN： 0021-9746 Impact factor: 3.411

11 in total

1. Thalassaemia in Britain.

Authors: S T CALLENDER; B J MALLETT; H LEHMANN
Journal: Br J Haematol Date: 1961-01 Impact factor: 6.998

2. A method for the estimation of the concentration of haemoglobin variants with particular reference to haemoglobins A2 and S and the recognition of thalassaemia minor.

Authors: H E HUTCHISON; P H PINKERTON; M AITON; P CASSIDY
Journal: Scott Med J Date: 1963-04 Impact factor: 0.729

9. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

Authors: K SINGER; A I CHERNOFF; L SINGER
Journal: Blood Date: 1951-05 Impact factor: 22.113

THALASSAEMIA IN SCOTS.

1. Thalassaemia in Britain.

2. A method for the estimation of the concentration of haemoglobin variants with particular reference to haemoglobins A2 and S and the recognition of thalassaemia minor.

3. Thalassemia in the West Indies.

4. Thalassaemia in an English and in a German family.

5. Haemoglobin Q-alpha-thalassaemia.

6. Thalassaemia minor in an English family.

7. A British target-cell anaemia.

8. The use of the isotope 51Cr as a label for red cells.

9. Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

10. The diagnosis of carriers of Cooley's anaemia.

1. Thalassaemia.

2. Haemoglobinopathies in immigrant families.

3. Thalassaemia in four generations of an English family.